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Companies: Let Us Know Your Key Personnel Needs
Jim Walkup, Vice President, Executive
Recruiter, BSBA from University of Alabama. Jim serves the
Pharmaceutical, Medical Device, Biotech and Health and
Beauty Aids Industries.
Jim recruits professional candidates,
management, R&D Technical, QC/QA, manufacturing,
engineering and other professionals for the above
industries.
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JOBS |
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Your resume is held in strict confidence,
all fees are employer paid, and relocation assistance is
provided for all qualified persons unless otherwise
stated.
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Updated February 2010
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QC HPLC Supervisor – 4 year science degree, prior management experience
in GMP lab. 5 years experience utilizing HPLC in lab. Supervise day-to-day
activities of HPLC analytical staff. Solid technical skills. Responsible for
all group functions: scheduling, testing, calibrations, instrument maintenance,
inventory control, training, methods development, validations and participated
hiring. Conducts research, quantitative and qualitative analysis and
experimentation. Pennsylvania. $50-60K
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Business Development Manager-Sales – Company expanding contract bottling
business of prescription, OTC and VMS products. B.S. 5+ years experience
developing contract packaging of pharmaceutical OTC and VMS sales and
distribution of products. Ability to develop new clients, both packaging
(bottling) and distribution (3PL) of product. Experience in soliciting and
closing new business and highly developed interpersonal and business negotiation
skills-proven track record. Set and meet quarterly and annual sales budgets. Charlotte, NC
area. Base salary depends on experience and knowledge, plus commission. |
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Sr. Process Engineer – Manager level. Biological Sterile Validation
Department. Process validation activities and principles for sterile and
vaccine manufacturing. Validation oversight of new product introductions and
new facility projects. Will serve as subject matter expert for Process
Validation which includes the development of strategies, standards,
requirements, tools and templates. BS, MS or PhD in Chemical Engineering,
biochemistry or comparable. Minimum 3 years direct responsibility for process
validation of biologics and minimum 5 years experience with biological
manufacturing processes. Pennsylvania. $90-125K. |
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R&D Quality Engineer – BS degree in Science or Engineering and 5 years in
Pharma industry in quality Assurance, Regulatory Affairs, or Quality R&D. this
job functions in the new products division of the nutraceutical products group
of this growing company. Will be responsible for ensuring documented compliance
of all applicable regulatory standards via generation, review and/or disposition
of all innovation quality documentation. Support new product development
activities. Design reviews and pre-validation assessment.
Charlotte,
NC. $70-75K base range, 8% bonus,
plus relocation. |
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Quality Assurance Compliance Manager – BA/BS. 6-10 years experience with
cGMP and regulated pharma industry practices: at least 6 years QA/Compliance, or
AA with 8-10 years of A/Compliance experience. Responsible for ensuring
compliance to GMP principles, leading and participating in investigations,
review/approval of process validation documents, and review/approval of
equipment and software qualification/validation documents to ensure compliance
with cGMPs, company procedures and regulatory commitments.
Florida.
$85-90K with bonus potential. Relocation will be provided with sign-on bonus.
Temporary living assistance available. |
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Quality Assurance Manager – BS/MS in life sciences and related
experience. Supervise and support all signed personnel. Assure that the
technical departments are properly staffed to complete required tasks. Evaluate
capital expenditures necessary to maintain or improve departmental operations.
Interface with FDA investigators and other government officials during plant
audits. Maintain relations with customers to aid in compliance with regulators,
or in development of new products. Assist during customer audits of facility.
ANDA, FDA, DEA. Florida. $50-60K. |
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CMS Project Management – BS with at least 5 years working experience as
project manager in GMP environment, pharma industry. PMP Certification
desired. Oversee all project management activities within the Chemistry and
Manufacturing Services department. These include the development and
optimization of project management systems within CMS to ensure communication
and transparency throughout the organization. The scope of the CMS project team
includes the transfer of technology form the Product Development group, pharma
process engineering, process scale-up, provides validation, building of launch
quantities and post-approval changes. Develop and optimize project management
systems to meet diverse needs of CMS. Manages project teams toward
implementation of the operational plan. PA. $115K + bonus + relo package. |
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QA/QC/Regulatory Affairs-Pharma – BS Chemistry. 2 years experience in
cGMP FDA regulated manufacturer. Responsible for providing quality support to
manufacturing, testing and releasing of products. Auditing, cGMP. Georgia. $70-80K. |
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Formulator Scientist – BS/MS pharma. Must have: 5-7 years formulation
experience in a pharma science or food technology and 2-4 years experience with
flavoring animal products or veterinary pharma. Participate in
multidisciplinary products development teams to advance early-stage development
compounds. Develop, design, balance flavor balance of veterinary application
products. SC. $50-85K – full relocation. |
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QC Supervisor – BS Technical. 2-5 years experience packaging of contract
pharma, OTC, VMS products. Must have QC packaging experience. Responsible for
interviewing, hiring, training, coaching personnel. Assure personnel follow
safety rules, GMPs. North Carolina. $50K+
depending on experience. |
Updated February 2010
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